ID

36848

Descrição

Two Doses of the Intravenous Magnesium Sulfate Versus the Standard Single Dose ,With/ Without the Nebulized Budesonide For the Management of the Severe Asthma Exacerbation in the Emergency Room; A Randomized Controlled Trial.; ODM derived from: https://clinicaltrials.gov/show/NCT02455687 Many studies have worked on the efficacy and safety of Intravenous magnesium sulfate and inhaled steroids beside the standard treatment for patients with severe asthma attacks. Investigators hypothesize that, two doses if intravenous magnesium sulfate with or without inhaled budesonide, would make the stay at the Pediatric emergency center (PEC) lesser,and decrease the need of being admitted to Pediatric Intensive Care Unit (PICU) for children with severe asthma attacks,compared to single dose of magnesium sulfate with or without inhaled budesonide.

Link

https://clinicaltrials.gov/show/NCT02455687

Palavras-chave

Versões (1)
  1. 15/06/2019 15/06/2019 -
Titular dos direitos

Hamad Medical Corporation

Transferido a

15 de junho de 2019

DOI

Para um pedido faça login.

Licença

Creative Commons BY-NC 3.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Magnesium Sulfate in Bronchial Asthma NCT02455687

Inglês

Eligibility Criteria

1 Formulários  
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
Is the participant a child of 2-14 years of age?
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
Is the participant known to have bronchial asthma?
Descrição

Bronchial asthma

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C0205309
Is the patient presenting in severe asthma exacerbation?
Descrição

Asthma exacerbation

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0205082
Does the particapant have a asthma severity score 8 or higher according to pram asthma severity?
Descrição

PRAM asthma score

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0581122
UMLS CUI [1,2]
C0449820
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
Does the participant have prematurity <34 weeks of gestation?
Descrição

Prematurity

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021294
Is the participant a critically ill child requiring immediate intubation or icu admission?
Descrição

Critically ill

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0175989
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0021925
UMLS CUI [2,1]
C0175989
UMLS CUI [2,2]
C1514873
UMLS CUI [2,3]
C0583239
Does the participant have transfers from other institutions?
Descrição

Transfer from other institutions

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1546432
UMLS CUI [1,2]
C0205394
Does the participant have an adverse drug reaction or allergy to budesonide, salbutamol, ipratropium bromide, prednisone, prednisolone, methylprednisolone, or magnesium sulfate?
Descrição

Adverse drug reaction

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0041755
UMLS CUI [1,2]
C0054201
UMLS CUI [2]
C0414042
UMLS CUI [3,1]
C0041755
UMLS CUI [3,2]
C0700580
UMLS CUI [4,1]
C0041755
UMLS CUI [4,2]
C0032952
UMLS CUI [5,1]
C0041755
UMLS CUI [5,2]
C0032950
UMLS CUI [6,1]
C0041755
UMLS CUI [6,2]
C0025815
UMLS CUI [7,1]
C0020517
UMLS CUI [7,2]
C0054201
UMLS CUI [8,1]
C0020517
UMLS CUI [8,2]
C0700580
UMLS CUI [9,1]
C0020517
UMLS CUI [9,2]
C0032952
UMLS CUI [10,1]
C0020517
UMLS CUI [10,2]
C0032950
UMLS CUI [11,1]
C0020517
UMLS CUI [11,2]
C0025815
UMLS CUI [12,1]
C0020517
UMLS CUI [12,2]
C0024480
Does the participant have a history of neuromuscular disease, cardiac disease, renal disease, liver disease?
Descrição

Neuromuscular, cardiac, renal or liver disease

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0027868
UMLS CUI [2]
C0018799
UMLS CUI [3]
C0022658
UMLS CUI [4]
C0023895
Does the participant have an underlying chronic lung disease.
Descrição

Chronic lung disease

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0746102
Does the participant have radiographic evidence of pneumonia or lung collapse?
Descrição

Pneumonia or lung collapse

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1711337
UMLS CUI [1,2]
C0032285
UMLS CUI [2,1]
C1711337
UMLS CUI [2,2]
C0004144
Does the participant have hemodynamic instability?
Descrição

Hemodynamic instability

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0948268
Does the participant have an instrumented airway or tracheotomy.
Descrição

Instrumented airway or tracheotomy

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0040590
UMLS CUI [1,2]
C0472567
Does the participant have colostomy or ileostomy.
Descrição

Colostomy or ileostomy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0009410
UMLS CUI [2]
C0020883
Does the participant have a malabsorption disorder?
Descrição

Malabsorption disorder

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0024523
Does the participant have a known vitamin D deficiency?
Descrição

Vitamin D deficiency

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0205309
UMLS CUI [1,2]
C0042870
Is the participant receiving milk of magnesium for constipation
Descrição

Milk of magnesium for constipation

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0026131
UMLS CUI [1,2]
C0024467
UMLS CUI [1,3]
C0009806
Does the participant have chronic diarrhea (duration for 2 weeks)?
Descrição

Chronic diarrhea

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0401151
Does the participant use diuretics?
Descrição

Diuretics

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0012798
Does the participant have immunodeficiency?
Descrição

Immunodeficiency

Tipo de dados

boolean

Alias
UMLS CUI [1]
C3829792
Voltar ao início da página

Similar models

Eligibility Criteria

1 Formulários
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
Is the participant a child of 2-14 years of age?
boolean
C0001779 (UMLS CUI [1])
Bronchial asthma
Item
Is the participant known to have bronchial asthma?
boolean
C0004096 (UMLS CUI [1,1])
C0205309 (UMLS CUI [1,2])
Asthma exacerbation
Item
Is the patient presenting in severe asthma exacerbation?
boolean
C0349790 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
PRAM asthma score
Item
Does the particapant have a asthma severity score 8 or higher according to pram asthma severity?
boolean
C0581122 (UMLS CUI [1,1])
C0449820 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Prematurity
Item
Does the participant have prematurity <34 weeks of gestation?
boolean
C0021294 (UMLS CUI [1])
Critically ill
Item
Is the participant a critically ill child requiring immediate intubation or icu admission?
boolean
C0175989 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0021925 (UMLS CUI [1,3])
C0175989 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0583239 (UMLS CUI [2,3])
Transfer from other institutions
Item
Does the participant have transfers from other institutions?
boolean
C1546432 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Adverse drug reaction
Item
Does the participant have an adverse drug reaction or allergy to budesonide, salbutamol, ipratropium bromide, prednisone, prednisolone, methylprednisolone, or magnesium sulfate?
boolean
C0041755 (UMLS CUI [1,1])
C0054201 (UMLS CUI [1,2])
C0414042 (UMLS CUI [2])
C0041755 (UMLS CUI [3,1])
C0700580 (UMLS CUI [3,2])
C0041755 (UMLS CUI [4,1])
C0032952 (UMLS CUI [4,2])
C0041755 (UMLS CUI [5,1])
C0032950 (UMLS CUI [5,2])
C0041755 (UMLS CUI [6,1])
C0025815 (UMLS CUI [6,2])
C0020517 (UMLS CUI [7,1])
C0054201 (UMLS CUI [7,2])
C0020517 (UMLS CUI [8,1])
C0700580 (UMLS CUI [8,2])
C0020517 (UMLS CUI [9,1])
C0032952 (UMLS CUI [9,2])
C0020517 (UMLS CUI [10,1])
C0032950 (UMLS CUI [10,2])
C0020517 (UMLS CUI [11,1])
C0025815 (UMLS CUI [11,2])
C0020517 (UMLS CUI [12,1])
C0024480 (UMLS CUI [12,2])
Neuromuscular, cardiac, renal or liver disease
Item
Does the participant have a history of neuromuscular disease, cardiac disease, renal disease, liver disease?
boolean
C0027868 (UMLS CUI [1])
C0018799 (UMLS CUI [2])
C0022658 (UMLS CUI [3])
C0023895 (UMLS CUI [4])
Chronic lung disease
Item
Does the participant have an underlying chronic lung disease.
boolean
C0746102 (UMLS CUI [1])
Pneumonia or lung collapse
Item
Does the participant have radiographic evidence of pneumonia or lung collapse?
boolean
C1711337 (UMLS CUI [1,1])
C0032285 (UMLS CUI [1,2])
C1711337 (UMLS CUI [2,1])
C0004144 (UMLS CUI [2,2])
Hemodynamic instability
Item
Does the participant have hemodynamic instability?
boolean
C0948268 (UMLS CUI [1])
Instrumented airway or tracheotomy
Item
Does the participant have an instrumented airway or tracheotomy.
boolean
C0040590 (UMLS CUI [1,1])
C0472567 (UMLS CUI [1,2])
Colostomy or ileostomy
Item
Does the participant have colostomy or ileostomy.
boolean
C0009410 (UMLS CUI [1])
C0020883 (UMLS CUI [2])
Malabsorption disorder
Item
Does the participant have a malabsorption disorder?
boolean
C0024523 (UMLS CUI [1])
Vitamin D deficiency
Item
Does the participant have a known vitamin D deficiency?
boolean
C0205309 (UMLS CUI [1,1])
C0042870 (UMLS CUI [1,2])
Milk of magnesium for constipation
Item
Is the participant receiving milk of magnesium for constipation
boolean
C0026131 (UMLS CUI [1,1])
C0024467 (UMLS CUI [1,2])
C0009806 (UMLS CUI [1,3])
Chronic diarrhea
Item
Does the participant have chronic diarrhea (duration for 2 weeks)?
boolean
C0401151 (UMLS CUI [1])
Diuretics
Item
Does the participant use diuretics?
boolean
C0012798 (UMLS CUI [1])
Immunodeficiency
Item
Does the participant have immunodeficiency?
boolean
C3829792 (UMLS CUI [1])
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial